List of works by Priit Palta

A comparison of the whole genome approach of MeDIP-seq to the targeted approach of the Infinium HumanMethylation450 BeadChip(®) for methylome profiling

scientific article

A molecular tool for menstrual cycle phase dating of endometrial samples in endometriosis transcriptome studies†

scientific article published on 01 July 2019

A parallel SNP array study of genomic aberrations associated with mental retardation in patients and general population in Estonia.

scientific article published on 26 November 2010

An expanded analysis framework for multivariate GWAS connects inflammatory biomarkers to functional variants and disease

scientific article published on 27 October 2020

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

scientific article published on 21 July 2015

Analysis of shared heritability in common disorders of the brain

scientific article published on 21 June 2018

Application of two different microarray-based copy-number detection methodologies – array-comparative genomic hybridization and array-multiplex amplifiable probe hybridization – with identical amplifiable target sequences

Array-MAPH: a methodology for the detection of locus copy-number changes in complex genomes

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published 16 May 2018 in Neuron

Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families

article by Padhraig Gormley et al published September 2018 in Neuron

Comparison of DNA extraction methods for multiplex polymerase chain reaction.

scientific article

Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms

scientific article published on 28 December 2016

Computational framework for targeted high-coverage sequencing based NIPT

scientific article published on 08 July 2019

Creating basis for introducing non-invasive prenatal testing in the Estonian public health setting

scientific article published on 06 November 2019

De novo mutations in schizophrenia implicate synaptic networks

scientific article

Detection of NASBA amplified bacterial tmRNA molecules on SLICSel designed microarray probes

scientific article

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization

Detection of tmRNA molecules on microarrays at low temperatures using helper oligonucleotides

scientific article

Distribution and medical impact of loss-of-function variants in the Finnish founder population

scientific article

Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations

scientific article published on 23 June 2017

Epigenetic DNA methylation changes associated with headache chronification: A retrospective case-control study

scientific article published on January 2017

Erratum: Corrigendum: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

scientific article published in October 2016

Evaluation of the 124-plex SNP typing microarray for forensic testing.

scientific article

Fluorescent labeling of NASBA amplified tmRNA molecules for microarray applications

scientific article published on 15 May 2009

Genetic analysis for a shared biological basis between migraine and coronary artery disease

scientific article published on June 2015

Genetic architecture of human plasma lipidome and its link to cardiovascular disease

scientific article published on 24 September 2019

Genome-wide meta-analysis identifies new susceptibility loci for migraine

scientific article

Genome-wide methylation analyses of primary human leukocyte subsets identifies functionally important cell-type-specific hypomethylated regions.

scientific article published on 24 October 2013

Haplotype phasing and inheritance of copy number variants in nuclear families

scientific article published on 8 April 2015

High-resolution population-specific recombination rates and their effect on phasing and genotype imputation

scientific article published on 28 November 2020

Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel

scientific article

Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa

scientific article

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

scientific article

NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies.

scientific article published on 4 April 2018

Screening of 20 patients with X-linked mental retardation using chromosome X-specific array-MAPH.

scientific article published on 29 September 2007

Structural genomic variation as risk factor for idiopathic recurrent miscarriage

scientific article

Systematic evaluation of NIPT aneuploidy detection software tools with clinically validated NIPT samples

scientific article published on 20 December 2021

TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting

scientific article published in 2018

The GENCODE exome: sequencing the complete human exome

scientific article

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom

scientific article published on February 2017

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